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Acrylic Acid (Industrial) - India
- Origin
- : India
- CAS Number
- : 79-10-7
- HS Code
- : 2916.11.00
Basic Info
- IUPAC Name
- : prop-2-enoic acid
- Molecular Formula
- : C3H4O2
- Molecular Weight (g/mol)
- : 72.0600
- Synonyms & Trade Names
- : Acrylic acid; Propenoic acid; Glacial acrylic acid
- Purity / Assay (%)
- : 99.5% min
- Grade / Quality Level
- : Industrial Grade
- Physical Form
- : Liquid
- Concentration
- : Pure substance
- Appearance / Color
- : Clear to slightly colored liquid
- Odor
- : Pungent, acrylic
- Melting Point (°C)
- : 14.0000
- Boiling Point (°C)
- : 141
- Density (g/cm³)
- : 1.0490
- Solubility in Water
- : Miscible
- Signal Word
- : Danger
- UN Number
- : 2218
- GHS Hazard Class
- : Flammable; Acute toxic; Skin corrosive; Respiratory sensitizer
- H-Statements
- : H226|H302|H312|H314|H317|H332|H335
- P-Statements
- : P210|P260|P264|P271|P272|P273|P280|P301+P330+P331
- REACH Status
- : Registered
- Drug Precursor Status
- : Non-precursor
- Storage Class (GHS)
- : 8
- Storage Conditions
- : Cool, dark; inhibitor required; away from peroxides
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Brief Overview
Acrylic acid, characterized by its unsaturated carboxylic acid structure (CH2=CHCO2H), presents as a clear, odorless liquid. It exhibits distinct solubility in water owing to its polar carboxylic acid functional group and mixes well with moderately polar organic compounds like alcohols, ethers, and chloroform. However, its sensitivity to air and water makes it highly reactive with free radicals, electrophilic or nucleophilic agents. Under specific conditions such as exposure to heat, light, or certain chemicals, acrylic acid tends to undergo polymerization, sometimes explosively, even at room temperature. This compound also displays corrosive properties towards metals and tissues.In various applications, acrylic acid finds use in multiple forms, including free acids, ammonium, and alkali salts. It serves diverse purposes such as thickening agents, dispersants, flocculants, wetting agents, coatings, and textile finishes. Its reactivity with a wide array of organic and inorganic compounds makes it a valuable source material for producing various lower molecular weight compounds. For instance, through reactions with water, alcohols, amines, halogens, and chlorinated hydrocarbons, acrylic acid can generate derivatives of propionic a
cid. Additionally, it participates in reactions leading to unsaturated fatty acids, heterocyclic compounds, and Diels-Alder addition products.
Due to its tendency to explosively polymerize, acrylic acid requires stabilization using inhibitors like hydroquinone before shipping. Typically, there's no need to remove the stabilizer as its effect can be balanced by adding an excessive initiator.
Manufacturing Process
he primary method embraced for producing acrylic acid involves the vapor-phase oxidation of propylene, a byproduct obtained during the production of ethylene and gasoline, into acrolein. Chemical-Grade (CG) propylene is commonly combined with steam and air in a two-stage oxidation process. Initially, propylene undergoes oxidation to form acrolein, which subsequently undergoes further oxidation to yield acrylic acid. These oxidation steps are conducted within tubular, fixed-bed reactors, utilizing the heat released by the exothermic reactions to generate steam.
